SIMRITE VERIFICATION AND SIMULATION SYSTEM— 510(k) K885081

Name: FDA 510(k) clearance K885081
Creator: U.S. Food and Drug Administration
Published: 1989-03-22

Substantially Equivalent

Haynes Radiation Ltd., Inc.

FDA 510(k) clearance K885081 for SIMRITE VERIFICATION AND SIMULATION SYSTEM, Substantially Equivalent on 1989-03-22. Applicant: Haynes Radiation Ltd., Inc.. Device class: 2.

Clearance details

Applicant: Haynes Radiation Ltd., Inc.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1988-12-09
Decision date: 1989-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alameda, CA, US

Download summary PDF View on FDA.gov ↗

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